Wikisage, the free encyclopedia of the second generation, is digital heritage

Cornelia de Lange Syndrome: Difference between revisions

From Wikisage
Jump to navigation Jump to search
No edit summary
 
(5 intermediate revisions by the same user not shown)
Line 1: Line 1:
{{disease|Q87.1|Cornelia de Lange Syndrome}}
{{disease|Q87.1|Cornelia de Lange Syndrome}}


Cornelia de Lange Syndrome (CdLS) is a very rare genetic disorder present from birth, but not always diagnosed at birth. It causes a range of physical, cognitive and medical challenges and affects both genders equally. The syndrome is named after Dutch pediatrician [[Cornelia de Lange|Cornelia Catharina de Lange]], who described it.<ref>https://en.wikipedia.org/w/index.php?title=Cornelia_de_Lange_Syndrome&oldid=677105911</ref><references/>
Cornelia de Lange Syndrome (CdLS) is a very rare genetic disorder present from birth, but not always diagnosed at birth. It causes a range of physical, cognitive and medical challenges and affects both genders equally. The syndrome is named after Dutch pediatrician [[Cornelia de Lange|Cornelia Catharina de Lange]], who described it.<ref>https://en.wikipedia.org/w/index.php?title=Cornelia_de_Lange_Syndrome&oldid=677105911</ref>
==Links==
 
{{wikidata|Q1133289}}
[http://www.ucdmc.ucdavis.edu/children/clinical_services/cleft_craniofacial/anomalies/cornelia.html Craniofacial anomalies – Cornelia de Lange Syndrome]
 
{{refs}}
 
[[Category:Medicine]]
[[nl:Cornelia de Lange]]

Latest revision as of 01:24, 29 August 2023

Disease classification WHO
Q87.1 Cornelia de Lange Syndrome

Cornelia de Lange Syndrome (CdLS) is a very rare genetic disorder present from birth, but not always diagnosed at birth. It causes a range of physical, cognitive and medical challenges and affects both genders equally. The syndrome is named after Dutch pediatrician Cornelia Catharina de Lange, who described it.[1]

Links

Q1133289 at Wikidata  Interwiki via Wikidata

Craniofacial anomalies – Cornelia de Lange Syndrome

References

References: